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Just a quick note to say hi!
You deserve a big bear hug!
You're in my thoughts all the time, but especially today.
Thank you for everything!
Welcome to our community!
You are in my thoughts and prayers.
Hope you feel better soon!
Congratulations! Time for a celebration...
Happy Birthday!
Avatar universal
05/11
You're in my thoughts all the time, but especially today. Terrie,, I will be praying for you , you deserve a break, and I want you to know that we are all here for you during this difficult time. Do you have other members of your family that you can go to for help? I would hate to see you have to go through this alone. You are not alone here though,
Love to you, and try to get some sleep!! :)
Stay strong and positive,
Pam
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Avatar universal
05/11
Thank you for your very kind message!! I wish you A LOT of luck in your fight against MS!!!!! It is tough, and that's why this forum is so great! Because you get to speak to people that are going through the same thing/s that you are or have. I like your profile name!! I tried using that, because I can't seem to stay asleep at all!! I belive I get 2ea. 2-3 hour streches a night. I've learned to live on it, but it would be SO NICE to get a full 6-8!!!! Again, Thank You for your kind words!! Stay positive, and stay HEALTHY!!!!
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Avatar universal
05/11
Just a quick note to say hi!
Terrie, I responded on my story journal but I also wanted to let you know that I am lucky to have good friends that care about me, whether you know me personally or not. We do have alot in common. I am on two doses of synthroid, .88 and .75 that I have to go back and forth with. It is so confusing sometimes. We all need to take a stand and bring our mystery stories to someone that will listen to us and not disregard what we know about our own bodies.
That's why my name is drs dont help, because so far,,,, none have!! LOL
Please have a wonderful day, you are in my thoughts and I will be there for you as well,
Hugs to you sweetie,
Pam
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Avatar universal
04/11
You're in my thoughts all the time, but especially today.
Terry, Please know that I am here for you if you need to vent or cry to or whatever... I know what you are going through and I just want you to know that you are not alone.
Hang in there, and don't give up.....

Big Hugs, Pam
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572651 tn?1530999357
03/11
I'm glad to see you are calling the doctor in the morning.  The swollen ankles is not a typical sign of MS. That is a sign that you might be having cirulatory problems.  That can easily come from some drugs - are you by any chance on any blood pressure meds?  Good luck with the doctor. -L
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Avatar universal
03/11
Just a quick note to say hi!  
Terrie, Thank you so much. The past 3 days have been very draining. Crying, laughing, story telling, and watching every single breath. She is a fighter. She is still hanging on. I can't imagine having to go through this with my mom or dad. It's horrible. My story about Angelina is in my journal. I hope she does know that I am there everyday for her. I love her and already missing her. They say that she has no brain activity and the only part of her brain that is functioning is for breathing and heartbeat. I can't believe it. I especially do not want her to live a life like that. She is basically a vegetable.
Anyway, it means alot to me that you are thinking about me and I am so sorry you had to go through this as well.
Hope you are doing well, Hugs,
Pam
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Avatar universal
03/11
Thank you. I am still waiting to hear that they took her off life support, she lost too much oxygen to her brain and is now braindead. It's hard to say goodbye when she is still alive, but really she isn't.
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198419 tn?1360242356
03/11
Good thing - I been through that can't sleep too, lol Glad your on something that helps!
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Avatar universal
03/11
Just a quick note to say hi!
Hi Terry, I know how agonizing the not knowing is. The hard part of it all is when you have a dx of Graves disease, alot of our problems that we have can get the drs. confused and blame it all on that. My eye disease is what is causing alot of confusion to them right now. I was dx'd with ischemic optic neuropathy, however, my opthalmologist told me that it will never get better, maybe stay stable or get worse. This is what is confusing.... my right  eye got really bad for 4 months, then started to get better by the 6th month. My vision was 20/70 in my right eye and then 6 months later is at 20/40. So is it ischemic optic neuropathy from graves eye disease or is it optic neuritis from ms?? No one has an answer.
Talk to ya soon, Pam
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Avatar universal
03/11
You deserve a big bear hug!
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198419 tn?1360242356
03/11
Welcome to our community! I don't sleep well either, lol! See you around soon! - shell
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Avatar universal
03/11
Just a quick note to say hi!
I believe I found my twin in you! Your story is verrrrrrrrry similar to mine.
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